Canonical Allele Identifier: PA179024
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile4184Ser
CA179023
NM_133432.3:c.12551T>G